CAS 4148-58-7
:a-D-Mannopyranoside, methyl4,6-O-(phenylmethylene)-
Description:
α-D-Mannopyranoside, methyl 4,6-O-(phenylmethylene)-, is a glycoside derived from D-mannose, a six-carbon aldose sugar. This compound features a pyranose ring structure, which is a six-membered ring containing five carbon atoms and one oxygen atom. The "4,6-O-(phenylmethylene)-" designation indicates that the hydroxyl groups at the 4th and 6th positions of the mannopyranoside are substituted with a phenylmethylene group, enhancing its reactivity and solubility properties. This modification can influence the compound's biological activity and interactions with other molecules. The presence of the methyl group at the anomeric carbon (C1) indicates that it is a methyl glycoside, which can affect its stability and reactivity in various chemical environments. The compound is typically used in synthetic organic chemistry and may serve as an intermediate in the synthesis of more complex carbohydrates or glycosides. Its CAS number, 4148-58-7, provides a unique identifier for regulatory and research purposes.
Formula:C14H18O6
Synonyms:- Mannopyranoside,methyl 4,6-O-benzylidene- (7CI)
- Mannopyranoside, methyl 4,6-O-benzylidene-, a-D- (8CI)
- Pyrano[3,2-d]-1,3-dioxin,a-D-mannopyranoside deriv.
- Methyl4,6-O-benzylidene-a-D-mannopyranoside
- Nsc 170162
- Methyl-4,6-O-(phenylmethylene)-alpha-D-mannopyranoside
- METHYL 4,6-O-BENZYLIDENE-A-D-MANNOPYRANOSIDE
- Methyl 4,6-O-Benzylidene-α-D-mannopyranoside
- Methyl 4,6-O-BenzylideneMannopyranoside
- METHYL 4,6-O-BENZYLIDENE-ALPHA-D-MANNOPYRANOSIDE
- METHYL-4,6-O-BENZYLIDEN-ALPHA-D-MANNOPYRANOSIDE
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
Methyl 4,6-O-benzylidene-a-D-mannopyranoside
CAS:<p>Methyl 4,6-O-benzylidene-a-D-mannopyranoside is a hexadecanoic acid that is mediated by the target cell. It has been shown to inhibit the growth of bacteria and cancer cells in vitro. Methyl 4,6-O-benzylidene-a-D-mannopyranoside also possesses an antibacterial activity with a low mammalian toxicity. This compound is hydrolyzed by esterases or glucuronidases, oxidized by cytochrome P450 enzymes, reduced by glutathione reductase, or conjugated with glucuronic acid. The residue of this compound has been shown to be carcinogenic in vivo and in vitro. Anticancer activity of this compound may be due to its ability to disrupt DNA synthesis and induce apoptosis of cancer cells.</p>Formula:C14H18O6Purity:Min. 95%Color and Shape:PowderMolecular weight:282.29 g/mol
